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Items: 1 to 20 of 209

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099210copy number variation1nstd231human GRCh38.p12 chr1: 66,256,800-84,953,993 , GRCh37 chr1: 66,722,483-85,419,676 ACADM, COX6A1P1, 211 more genes
    nsv7057605inversion1nstd229human GRCh38 chr1: 78,336,704-86,162,072 , GRCh37.p13 chr1: 78,802,388-86,627,755 LINC01712, LOC105378812, 74 more genes
    nsv7057036inversion1nstd229human GRCh38 chr1: 81,424,308-84,666,974 , GRCh37.p13 chr1: 81,889,993-85,132,657 SSX2IP, LINC01361, 29 more genes
    nsv7053103inversion1nstd229human GRCh38 chr1: 81,888,908-86,483,944 , GRCh37.p13 chr1: 82,354,593-86,949,627 C1orf52, DNAI3, 50 more genes
    nsv7046575inversion1nstd229human GRCh38 chr1: 83,069,893-89,051,563 , GRCh37.p13 chr1: 83,535,576-89,517,246 LOC105378826, RN7SL583P, 87 more genes
    nsv7045562inversion1nstd229human GRCh38 chr1: 82,773,087-84,647,821 , GRCh37.p13 chr1: 83,238,770-85,113,504 LOC107985396, LINC01362, 22 more genes
    nsv7041571inversion1nstd229human GRCh38 chr1: 84,455,419-86,210,703 , GRCh37.p13 chr1: 84,921,102-86,676,386 GNG5, DNAI3, 25 more genes
    nsv6656332copy number variation1nstd229human GRCh38 chr1: 84,685,373-84,686,149 , GRCh37.p13 chr1: 85,151,056-85,151,832 SSX2IP
    nsv6656160copy number variation1nstd229human GRCh38 chr1: 84,403,990-84,767,957 , GRCh37.p13 chr1: 84,869,673-85,233,640 GNG5, SPATA1, 7 more genes
    nsv6656155copy number variation1nstd229human GRCh38 chr1: 84,297,101-85,026,300 , GRCh37.p13 chr1: 84,762,784-85,491,983 LOC102724892, MCOLN3, 13 more genes
    nsv6655921copy number variation1nstd229human GRCh38 chr1: 84,679,275-84,684,362 , GRCh37.p13 chr1: 85,144,958-85,150,045 SSX2IP
    nsv6655920copy number variation1nstd229human GRCh38 chr1: 84,669,768-84,676,252 , GRCh37.p13 chr1: 85,135,451-85,141,935 SSX2IP
    nsv6655919copy number variation1nstd229human GRCh38 chr1: 84,636,001-84,643,200 , GRCh37.p13 chr1: 85,101,684-85,108,883 SSX2IP
    nsv6626479copy number variation1nstd224human GRCh37 chr1: 85,044,425-85,153,076 , GRCh38.p12 chr1: 84,578,742-84,687,393 LINC01461, SSX2IP, 2 more genes
    nsv6329140copy number variation1nstd223human GRCh38 chr1: 84,665,847-84,667,284 , GRCh37.p13 chr1: 85,131,530-85,132,967 SSX2IP
    nsv6320541copy number variation1nstd223human GRCh38 chr1: 84,673,601-84,675,300 , GRCh37.p13 chr1: 85,139,284-85,140,983 SSX2IP
    nsv6319474copy number variation1nstd223human GRCh38 chr1: 84,669,050-84,669,658 , GRCh37.p13 chr1: 85,134,733-85,135,341 SSX2IP
    nsv6315730copy number variation1nstd223human GRCh38 chr1: 84,686,801-84,692,700 , GRCh37.p13 chr1: 85,152,484-85,158,383 SSX2IP
    nsv6313574copy number variation1nstd102humanPathogenic GRCh37 chr1: 68,180,293-92,731,957 , GRCh38.p12 chr1: 67,714,610-92,266,400 RNA5SP51, ADGRL4, 315 more genes
    nsv5984962copy number variation1nstd212human GRCh38 chr1: 84,677,087-84,859,877 , GRCh37.p13 chr1: 85,142,770-85,325,560 LPAR3, SSX2IP, 1 more genes
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